ZMP
si:ch211-197g15.13
Ensembl ID:
ZFIN ID:
Description:
LOC798876 protein [Source:UniProtKB/TrEMBL;Acc:A8KB45]
Human Orthologue:
PIP5K1C
Human Description:
phosphatidylinositol-4-phosphate 5-kinase, type I, gamma [Source:HGNC Symbol;Acc:8996]
Mouse Orthologue:
Pip5k1c
Mouse Description:
phosphatidylinositol-4-phosphate 5-kinase, type 1 gamma Gene [Source:MGI Symbol;Acc:MGI:1298224]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45766 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa24142 | Nonsense | Available for shipment | Available now |
| sa3152 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa45766
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060786 | Nonsense | 308 | 682 | 7 | 18 |
| ENSDART00000105443 | Nonsense | 269 | 633 | 6 | 17 |
| ENSDART00000111931 | None | None | 274 | None | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 17789647)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 17540582 |
| GRCz11 | 22 | 17565560 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGACTCATGCTGGACACAGACACATACAACGCCCTGGTCAAGACCTTA[C/T]AGAGAGACTGTTTGGTAAGTTCTGGACAGGACAAAACATTTGAACCAGAT
Long Flanking Sequence:
CATTTAAGAAAAAATGAAAGGGCTCTTCTTCACCTTAAATCCAAAATTGTATTGTGAGATTAATATTGTGAATCGCATTGCATCGTGAGTCAGGTGAATCGTTACATCCCTGTTCGCAAACCATGTAATCAACAAATACAAGTATAAATCATTTAGCACAGCGTATTTGTTTACATCTGCTAGTCGTTTAATCTTTCAAATGTTTGTCTCCTCAGAACTTGAATCAGAATCCTCGCACCTTATTACCCAAGTTCTTCGGGCTCTACTGCGTACAATCGGGTGGCAAGAACATTCGAATGGTGGTGATGAACAACGTTTTGCCCAGGGTGGTGCGCATGCACCTTAAATACGACTTAAAGGGGTCCACATACAAAAGGCGGGCATCAAAAAAAGAACGGGAAAAGGCAAAACCAACTTTTAAAGACCTTGACTTCATGCAGGAATTACCAGACGGACTCATGCTGGACACAGACACATACAACGCCCTGGTCAAGACCTTA[C/T]AGAGAGACTGTTTGGTAAGTTCTGGACAGGACAAAACATTTGAACCAGATAAATGTTTGTAATGAGTAGGATTTTAAAGATATTTTTGAAGCTGTTCTGCTCAACAAGGCTGCATTAATTTGATCAAAAATACAGTAAAAATGTGAAACATGATTACAGTTTAAAATAAGTGCTTCCCTATTTAATGTAGTTAAAAACTGTCCTTATTCCTGATTTAAAGCTACACTTTCACTATCATTACTTCCGTCTTCAGGTGTCGCATGAATCTTTGGAAATGATTATAATATTATGATCTGCTGTTCAATAAATATTAGTTAATTTCTTGCATTTATACAGCGCTTTTCTAGACAATCAAAGCGCTTTACACAATAACGGGAATCTCCTCATCCACCACCAGTGTGCAGCATCCAACTGGATGACACAACAGCAGCCAAATTGCGCCAGACCGTGCACCCCACAACAGCTAATTGATGGAGAGAAGACAGAGTGATAAAGCCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24142
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060786 | Nonsense | 636 | 682 | 16 | 18 |
| ENSDART00000105443 | Nonsense | 587 | 633 | 16 | 17 |
| ENSDART00000111931 | None | None | 274 | None | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 17774726)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 17525661 |
| GRCz11 | 22 | 17550639 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATCGTGGTGGAGTCTGACGGCGGCAGTCAGGCCTCAGGCTGTACAAGT[A/T]GAGCCTCGGTGGACGAGGAGGATGACGTGCCAATCACAGACATTTATTTT
Long Flanking Sequence:
TGGTTTGTGGTGTGCGGTCGGCCATCACATCATTTAGTTGGAGACTGCACACTGGTGGGGAATGAGAATCCCCGCAATGTGTAAAGCGCTTTTAGTATCTAGAAAAGCTCTATATAAGTGTAAGGAATTATAATTATGTCAATTTTATAATCCAGACTAAAAACAACTAACTAAAACAAAAGCCAAATATTAATGAACACTATAATATATAATTAATGGTACAATTACACTTCCAAAGAGACTCATAAAATTTTGAGTATGTTTTTACCAAAACAAAGAAGAAAAGATAAAATTAGTTCCATTTCAACTTCATTTGACAGTTTTGCCAGATGAACAGGCAACATTATACTCCCTGATGATCTCAAAACAATGTTTCTGTTTGTCGTGTGTCCAGTGAAGCTGCAGAGACTATTCCAGAAGCCTCGTCCTCCTCCGTCCCGGCGAGTCCCAGGATCGTGGTGGAGTCTGACGGCGGCAGTCAGGCCTCAGGCTGTACAAGT[A/T]GAGCCTCGGTGGACGAGGAGGATGACGTGCCAATCACAGACATTTATTTTGTAAGCTGATCAATTTAACCAGACATATCTTCAAACATGCAAACATTTAATTTTTCATTTTAAAAGTAAGTTTCCTTGAGAGCTTGGACATGAAATAAATATAAATATATAGAATCACTCACACTTTGCAATAAGTTGCTTAATGCATTCACAAACATGAACTAATAATGAACAATACTTGTACAGCCTAAATGAATCACAGTTCAACATTTACTAATGCGTTATTAAAAACTGAATTTTTATTTGTCATCAGTACACTGTTAGCTAACATGAACTAACAGTGAACAACTCTATTTTCATTAACTAACATGAAGAAATACTGTAATCAATATATTGTTTATTGTTTGTTCGTGTTAGTAAGTGCACAACATAACTAATACAACCTAAGTTACCTACGTTTCTTCTAACATAGTAAATTTACTTAAAGTACAGTTAAATGTAAGCTTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3152
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060786 | Nonsense | 675 | 682 | 17 | 18 |
| ENSDART00000105443 | Nonsense | 626 | 633 | 17 | 17 |
| ENSDART00000111931 | None | None | 274 | None | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 17768162)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 17519097 |
| GRCz11 | 22 | 17544075 |
KASP Assay ID:
554-2472.1 (used for ordering genotyping assays)
KASP Sequence:
GCTGGGTTTATTCTCCTCTGCATTTCAGCTCAGGGCCTAAAACCCTGCCC[G/T]AGGATGAAGGGGAAAGTGAAACAGTAAGTGTGCATTGTGTCATTSATCGT
Long Flanking Sequence:
TAATGTCCATCTCTAGCCACTGTGTTTTTAAAGGTTTTGTTTACATGGCAGTGGTGCACATGCAAATTTCGCTTTTAAATGTTTGAATTTTTTTACACGCAATAAACTAATTGCACTCTATTCCGTATCCCAGGCCAGTAGATGGCGACTTCACTTCGTAAATAAACACCAATAATCTGTGCACAGATGTAGTCGTTCTAGTATGTGAAGGTGACTATAGACTGAAGGCTTTTACATTGGTTTTTTTATATAGTTAAAATAAAGATGTTTTAGTAGTTTAGCTTTCAAATAACGTGTACTTCAAAACCCATTTCCATTTTCCCGACACCTTGAAATGTTCAAATCGGTGACACTTATATTCCTCTCTGCCGCTCTTGTTTTCCTGTCTTTCCTCCTCTCTGGCTCCCTCTGCTGTACTGCTGGTATAACTGCAGCCTCCAGAAGACAAAAGCTGGGTTTATTCTCCTCTGCATTTCAGCTCAGGGCCTAAAACCCTGCCC[G/T]AGGATGAAGGGGAAAGTGAAACAGTAAGTGTGCATTGTGTCATTGATCGTCTTCAGTTCACAGTCCTTGATGTTGATGGTAGCAACCCTTTTTACCATGTCTCGACAGTAATCAGACCTCAGGAGAGAAGGGCAGCTAAAGGTTTGGACTCTTCAGATGAATCATGTCGGATGGACGCTGCTGTCAGATGTTTCCGCAACTGCTTCATCTTCATCGTCCTGTCATCTATTCCACAAACAGAACCAAGCGAGTGGTAATGCCATTGTATAGAGGTATTTAAAAGTAATAATGAAAGTTTTTGTTTGATTGTGTTAAAAGTTCTGTTCTTTTATTTTATTAAGTACTGTGAAATGTGTTCATCCAAGTAAGTTCTGGGACTCAAGCCTCTCCTCATTGGCATTTTTTTTATTTTTTTTATTTTGGAGGTAGGCTGAGAGTTTTGTTGACAAAATAAATGTATTTGTATTTATTTTAGTTTGGTTATTGGCATCATTACGAAA
Associated Phenotype:
Not determined